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Cardiac Rehabilitation and Metabolomics in Heart Failure (CROMe)

Primary Purpose

Heart Failure

Status
Completed
Phase
Not Applicable
Locations
Kenya
Study Type
Interventional
Intervention
Integrated cardiac rehabilitation
Usual Care
Sponsored by
Duke University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Heart Failure focused on measuring rehabilitation, metabolomics

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. NYHA Class II or III heart failure
  2. Owns a mobile telephone
  3. Can participate in supervised exercise three times a week
  4. Can read/ primary care giver can read in English or Kiswahili

Exclusion Criteria:

  1. Recent acute illness requiring hospitalization in the preceding 4 weeks.
  2. Limitation of activity because of factors other than fatigue or exertional dyspnea, such as arthritis, claudication in the legs, angina, advanced co morbidities.
  3. Known uncontrolled arrhythmia.
  4. Heart failure due to congenital heart disease.
  5. Pregnant patients as may be confirmed by patient report or urine pregnancy tests
  6. Heart failure due to obstructive cardiomyopathy including mitral stenosis and aortic stenosis.
  7. Use of pacemakers.

Sites / Locations

  • Moi teaching and Referral Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Integrated cardiac rehabilitation

Usual Care

Arm Description

Participants enrolled in integrated cardiac rehabilitation plus usual care

Participants receiving usual care only

Outcomes

Primary Outcome Measures

6 minute walk time distance
This study seeks to find out whether 6 minute walk time distance among patients undergoing integrated cardiac rehabilitation is different when compared to usual care study participants.

Secondary Outcome Measures

Depression severity
Change in total depression screening scores using PHQ9 score
Quality of living
Change in quality of living total score as measured by the WHO quality of life scale.

Full Information

First Posted
November 14, 2018
Last Updated
November 25, 2019
Sponsor
Duke University
Collaborators
Moi Teaching and Referral Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03743012
Brief Title
Cardiac Rehabilitation and Metabolomics in Heart Failure
Acronym
CROMe
Official Title
Cardiac Rehabilitation Outcomes and Metabolomic Profiles Among Patients With Heart Failure in Western Kenya
Study Type
Interventional

2. Study Status

Record Verification Date
November 2019
Overall Recruitment Status
Completed
Study Start Date
November 1, 2018 (Actual)
Primary Completion Date
October 31, 2019 (Actual)
Study Completion Date
October 31, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Duke University
Collaborators
Moi Teaching and Referral Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a randomized controlled trial of participants with heart failure randomized into usual care plus integrated cardiac rehabilitation or usual care only. The rehabilitation protocol will comprise one month of thrice weekly sessions including supervised aerobic exercises and counseling, followed by two months of monitored home based exercises prescribed weekly. Cardiopulmonary performance status, depression and quality of life will be assessed at enrollment and upon completion of the protocol using the 6-minute walk time distance test. Plasma samples will be collected and bio-banked for metabolomic profiling and comparative outcome analysis.
Detailed Description
Integrated cardiac rehabilitation will comprise one month of thrice weekly sessions of supervised aerobic exercises and counseling, followed by two months of monitored home based exercises prescribed weekly. Aerobic threshold (AT) will be determined based on perceived rates of exertion as measured using a Borg scale and target heart rate based on Karvonen's formula. Exercise intensity will be prescribed to achieve the earlier of moderate perceived exertion and 50-60% of their maximal target heart rate on a treadmill. Intensity will be increased over the course of the 12 sessions to attain 70-80% of maximal target heart rate. Duration of exercise will also be increased gradually over the 12 sessions in keeping with the study participants perceived rate of exertion. Participants will be given pedometers and instructed to use these daily for the period of the study. At the end of the first four weeks, the participant's weekly steps will be averaged to establish a baseline weekly step target. Starting in the 4th week,subjects will be instructed to continue exercises at home whilst maintaining a comparable activity level as will be measured by their weekly step counts. Participants will be contacted weekly for the remaining 8 weeks and step targets will be prescribed based on 10% weekly increments.Prior to the start of each exercise session, participants will receive a brief counseling module reflecting the primary goals of cardiac rehabilitation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure
Keywords
rehabilitation, metabolomics

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
91 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Integrated cardiac rehabilitation
Arm Type
Experimental
Arm Description
Participants enrolled in integrated cardiac rehabilitation plus usual care
Arm Title
Usual Care
Arm Type
Active Comparator
Arm Description
Participants receiving usual care only
Intervention Type
Other
Intervention Name(s)
Integrated cardiac rehabilitation
Intervention Description
Participants enrolled to the integrated cardiac rehabilitation arm will participate in individually tailored rehabilitation sessions that will involve aerobic activity focused on exertion at the participant's aerobic threshold (AT) over a duration of three months.
Intervention Type
Other
Intervention Name(s)
Usual Care
Intervention Description
Participants randomized to the usual care arm will be instructed on the benefits of exercise and continue with usual care. Participant activity will be tracked monthly using pedometers for three months of follow up.
Primary Outcome Measure Information:
Title
6 minute walk time distance
Description
This study seeks to find out whether 6 minute walk time distance among patients undergoing integrated cardiac rehabilitation is different when compared to usual care study participants.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Depression severity
Description
Change in total depression screening scores using PHQ9 score
Time Frame
3 months
Title
Quality of living
Description
Change in quality of living total score as measured by the WHO quality of life scale.
Time Frame
3 months
Other Pre-specified Outcome Measures:
Title
Metabolomic Profile
Description
This study will secondarily describe pre - post intervention changes in metabolomic profiles in participants with heart failure as measured using mass spectroscopy
Time Frame
3 months
Title
Inflammatory Profile
Description
This study will secondarily describe pre - post intervention changes in markers of inflammation such as hsCRP, interleukin-6, TNF-α, and ICAM-1 in participants with heart failure.
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: NYHA Class II or III heart failure Owns a mobile telephone Can participate in supervised exercise three times a week Can read/ primary care giver can read in English or Kiswahili Exclusion Criteria: Recent acute illness requiring hospitalization in the preceding 4 weeks. Limitation of activity because of factors other than fatigue or exertional dyspnea, such as arthritis, claudication in the legs, angina, advanced co morbidities. Known uncontrolled arrhythmia. Heart failure due to congenital heart disease. Pregnant patients as may be confirmed by patient report or urine pregnancy tests Heart failure due to obstructive cardiomyopathy including mitral stenosis and aortic stenosis. Use of pacemakers.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gerald Bloomfield, MD
Organizational Affiliation
Duke University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Felix Barasa
Organizational Affiliation
Moi Teaching and Referral Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Moi teaching and Referral Hospital
City
Eldoret
State/Province
Uasin Gishu
ZIP/Postal Code
30100
Country
Kenya

12. IPD Sharing Statement

Plan to Share IPD
No
Links:
URL
https://clinicaltrials.gov/ct2/show/NCT02795936
Description
Feasibility study

Learn more about this trial

Cardiac Rehabilitation and Metabolomics in Heart Failure

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